Synthesis and self-assembling behavior of a porphyrin bearing multiple meso-conjugated barbiturates

被引:3
|
作者
Arai, Satoshi [1 ]
Okamura, Toshiya [1 ]
Takeoka, Shinji [1 ]
机构
[1] Waseda Univ, Dept Life Sci & Med Biosci, Fac Sci & Engn, Shinjuku Ku, Tokyo 1628480, Japan
关键词
Porphyrin; Hydrogen bonding; Self-assembly; Barbituric acid; MOLECULAR RECOGNITION; SCHIFF-BASES; ACID; DERIVATIVES; WATER; TAUTOMERISM; COMPONENTS; FILM;
D O I
10.1016/j.tetlet.2010.07.139
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
An efficient procedure through deprotection of 2,4,6-trimethoxypyrimidine derivative afforded porphyrinato zinc bearing multi-barbiturates acting as multiple hydrogen bonding sites at the meso positions. Addition of excess amphiphilic triaminopyrimidine derivative, as a complementary motif to the barbiturate, in an aqueous solution of porphyrin conjugated with multiple barbiturates at the meso positions resulted in precipitation. The cast film from the chloroform solution of the precipitate indicated the formation of a well-defined porphyrin assembly. (c) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5177 / 5180
页数:4
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